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UROD encodes an enzyme in the heme biosynthetic pathway. Zusätzlich bieten wir Ihnen Uroporphyrinogen Decarboxylase Antikörper (67) und Uroporphyrinogen Decarboxylase Kits (3) und viele weitere Produktgruppen zu diesem Protein an.
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Human UROD Protein expressed in Escherichia coli (E. coli) - ABIN667032
Garey, Hansen, Harrison, Kennedy, Kushner: A point mutation in the coding region of uroporphyrinogen decarboxylase associated with familial porphyria cutanea tarda. in Blood 1989
Zeige alle 2 Referenzen für ABIN667032
a new mutation in the UROD gene in Egyptian patients with Hepatoerythropoietic porphyria, is reported.
a new insight in the conformational changes occurred in the mutant structures of UROD protein.
Data suggest that the traditional Chinese medicine (TCM) candidate potential three-in-one inhibitors for three drug target proteins epidermal growth factor receptor (EGFR (zeige EGFR Proteine)), Her2 (zeige ERBB2 Proteine), and uroporphyrinogen decarboxylase (UROD) against head and neck cancer.
Expression of the D306Y mutation results in an insoluble recombinant protein. G318R and K297N have little effect on the structure or activity of recombinant URO-D, but the proteins display reduced stability in vitro.
Among seventeen F-PCT patients, sixteen UROD mutations were identified.
analysis of uroporphyrinogen decarboxylase as a potential target for specific components of traditional Chinese medicine
Mutations in UROD gene is associated with familial porphyria cutanea tarda.
Hepatoerythropoietic porphyria and familial porphyria cutanea tarda G281E mutation in the uroporphyrinogen decarboxylase gene
function of Arg37 in uroporphyrinogen III decarboxylase
description of 3 siblings with hepatoerythropoietic porphyria; sequencing of the UROD gene revealed compound heterozygosity for a novel missense mutation, V166A, and a complex deletion/insertion, 645del1053ins10
This gene encodes an enzyme in the heme biosynthetic pathway. This enzyme is responsible for catalyzing the conversion of uroporphyrinogen to coproporphyrinogen through the removal of four carboxymethyl side chains. Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoetic porphyria.
, protein UroD
, Uroporphyrinogen decarboxylase
, uroporphyrinogen III decarboxylase
, porphyrinogen carboxylase